期刊名称：Health Psychology and Behavioral Medicine: An Open Access Journal
电子版ISSN：2164-2850
出版年度：2021
卷号：9
期号：1
页码：380-397
DOI：10.1080/21642850.2021.1918552
出版社：Taylor and Francis Ltd
摘要：Background Dialysis implies huge changes in patients’ lives. Yet, there is a need to better understand patients’ experience in the time following dialysis initiation. Objective The objective of this study was to investigate patients’ experience of dialysis a year after treatment initiation and the associations between patients’ discourse and their anxiety and depression symptoms. Methods Twenty two patients (mean age 63.4; 68% men) took part in a semi-directed interview about their experience with dialysis. Participants completed the Hospital Anxiety and Depression Scale (HADS). Interviews were analyzed using a lexicometric analysis. Results The analysis generated five classes: experience with nephrological care, facing loss and family relationships, family and acceptance, implementation of a new routine and making sense of the end-stage renal disease experience. Patients’ felt very passive in their experience with care. They reported the importance of integrating dialysis in their lives and the role of family support when facing treatment initiation. Depressed patients were more likely to describe their nephrological monitoring very factually and to talk about what they lost with dialysis initiation. Conclusion Dialysis initiation is a hard time for patients during which they face many challenges. This first year represents a time of adaptation, in which family seems essential.
